Researchers at the University of California Santa Barbara say they have designed a nanoparticle that has several important properties. Spherical in shape and silver in composition, it is encased in a shell coated with a peptide that enables it to target tumor cells, they explain.
What's more, the shell is etchable so those nanoparticles that don't hit their target can be broken down and eliminated. The research findings (“Etchable plasmonic nanoparticle probes to image and quantify cellular internalization”) appear in Nature Materials.
The core of the nanoparticle employs a phenomenon called plasmonics whereby nanostructured metals such as gold and silver resonate in light and concentrate the electromagnetic field near the surface. In this way, fluorescent dyes are enhanced, appearing about tenfold brighter than their natural state when no metal is present. When the core is etched, the enhancement goes away and the particle becomes dim.
UCSB’s Ruoslahti Research Laboratory also developed a simple etching technique using biocompatible chemicals to rapidly disassemble and remove the silver nanoparticles outside living cells. This method leaves only the intact nanoparticles for imaging or quantification, thus revealing which cells have been targeted and how much each cell internalized.
“The disassembly is an interesting concept for creating drugs that respond to a certain stimulus,” said Gary Braun, Ph.D., a postdoctoral associate in the Ruoslahti Lab in the department of molecular, cellular, and developmental biology and at Sanford-Burnham Medical Research Institute. “It also minimizes the off-target toxicity by breaking down the excess nanoparticles so they can then be cleared through the kidneys.”
This method for removing nanoparticles unable to penetrate target cells is unique. “By focusing on the nanoparticles that actually got into cells,” Dr. Braun said, “we can then understand which cells were targeted and study the tissue transport pathways in more detail.”
“We present a class of multicolored plasmonic nanoprobes comprising dye-labeled AgNPs that are exceptionally bright and photostable, carry peptides as model targeting ligands, can be etched rapidly and with minimal toxicity in mice, and that show tumor uptake in vivo,” wrote the investigators.
Some drugs are able to pass through the cell membrane on their own, but many drugs, especially RNA and DNA genetic drugs, are charged molecules that are blocked by the membrane. These drugs must be taken in through endocytosis, the process by which cells absorb molecules by engulfing them.
“This typically requires a nanoparticle carrier to protect the drug and carry it into the cell,” continued Dr. Braun said. “And that's what we measured: the internalization of a carrier via endocytosis.”
Because the nanoparticle has a core shell structure, the researchers can vary its exterior coating and compare the efficiency of tumor targeting and internalization. Switching out the surface agent enables the targeting of different diseases—or organisms in the case of bacteria—through the use of different target receptors. According to Dr. Braun, this should turn into a way to optimize drug delivery where the core is a drug-containing vehicle.